Looking for a CRO that can deliver quality statistical output? ✅ At PharPoint, ensuring quality starts early, with collaboration both within and across functional areas to identify the best leads and team members suited for a project and the scheduling of an effective kick-off meeting. Once a project moves to the programming phase, the below processes help ensure quality:👇
PharPoint Research, Inc.
Research Services
Durham, NC 17,363 followers
We're a contract research organization (CRO) that helps innovative clients meet their clinical trial goals.
About us
PharPoint Research is an award-winning, client-focused contract research organization (CRO) with offices in the Research Triangle Park and Wilmington, NC. We provide nimble drug development solutions to clients of all sizes and have supported over 1,000 studies since 2007. PharPoint's services include: clinical operations, project management, data management, medical monitoring, biostatistics, statistical programming, medical writing, and study rescue. ---- RECRUITMENT FRAUD ALERT: Unsuspecting job seekers have reported receiving unsolicited contacts by phone, email, text, online recruitment services (including LinkedIn) and bogus websites from individual(s) purporting to be or represent PharPoint recruiters. Be advised that PharPoint does not extend unsolicited employment offers and all candidates must go through a formal interview process to be considered for an offer of employment. Full statement: https://pharpoint.com/careers/recruitment-fraud-alert/
- Website
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http://pharpoint.com
External link for PharPoint Research, Inc.
- Industry
- Research Services
- Company size
- 51-200 employees
- Headquarters
- Durham, NC
- Type
- Privately Held
- Founded
- 2007
- Specialties
- Clinical Data Management, Biostatistics, Project Management, Clinical Monitoring, Statistical Programming, Medical Writing, and Medical Monitoring
Locations
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Primary
5003 South Miami Blvd
Suite 100
Durham, NC 27703, US
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1001 Military Cutoff Rd
Suite 301
Wilmington, NC 28405, US
Employees at PharPoint Research, Inc.
Updates
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What does an effective Data Monitoring Committee (DMC) Charter look like? In our latest blog post, we spoke with PharPoint's Sr. Project Specialist and experienced DMC Coordinator, Victoria, for insight, discussing things like: 📝 Typical charter length 👋 How a study partner (like PharPoint!) can help 💼 What the FDA's latest guidance says about DMC charter contents Read more: https://lnkd.in/eWVMcxdc #ClinicalTrials #DataMonitoringCommittee
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An effective, comprehensive clinical development plan (CDP) is typically quite robust, requiring a consultative multidisciplinary team to pull together - and one of the key sections within your CDP should include information regarding the clinical trials you'll need for market approval. What information is contained in this section? The below five areas are a great place to start. (👋 Looking for some extra support from an experienced clinical consultant? We'd love to chat. Head to the PharPoint website to reach out to our team.)
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How can early engagement with an experienced biostatistician help you build out a strong study framework and ensure your trial is designed to produce meaningful results? Read the latest article (including our team's insight on three critical qualities to look for an a biostatistics consultant 👀) in our Resource Library: https://lnkd.in/e22gbm3u
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As you progress in your career, experience and time can help you determine what matters most to you in a workplace (and there's no one right answer!). For PharPoint Principal Data Manager Shantyana, a great team and an environment conducive to learning and visibility are some of the key ingredients to an enjoyable workplace — all qualities she's found here in her time at PharPoint. Get to know Shantaya, her experience working at PharPoint and her career path in this month's #MeetThePharPointTeam article: https://lnkd.in/ewt3z5Y4 #LifeatPharPoint
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Sr. Recruiter Cameron Bullman is back with the latest edition of "CRO Career Insights"! In this issue, he discusses the importance of maintaining a work-life balance and the many ways you can achieve it. #LifeatPharPoint #lifesciences #clinicalresearch
CRO Career Insights | PharPoint Research - Vol. 6
PharPoint Research, Inc. on LinkedIn
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What is a biostatistician's role in supporting a successful regulatory submission, and how can a CRO with a strong biostatistics team help a sponsor confidently navigate regulatory discussions? In our latest blog post, we discuss: ✅ Delivering high-quality, FDA compliant regulatory submissions ⛔ The impact of an unsatisfactory submission 🙋 How early biostatistician interaction can support better submissions Read the full article here: https://lnkd.in/eKBW854P
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As a Lead Data Manager, PharPoint's Alyssa L. works very closely with clients, ensuring all DM deliverables are met on time and communication with clients is clear and effective. In our latest #MeetThePharPointTeam article, Alyssa shared details on her career journey, including how having a supportive team around her has helped her grow her career within data management. Get to know Alyssa and learn more about what it's like to work within data management at PharPoint: https://lnkd.in/erd9JeTC #LifeatPharPoint
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PharPoint Research, Inc. reposted this
Data monitoring committees (DMCs) are more commonly used in trials today than in years past, but has the availability of DMC-experienced clinicians to staff those committees kept up? In a new article on our website, we looked at relevant industry guidance and publications and spoke with an experienced DMC coordinator to discuss the growth of DMCs compared to the growth of potential DMC members, the industry outlook on member training, and the components of an effective DMC training session. Get the details: https://lnkd.in/eVkJjx2k
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